'under dissolution' is correct and usable in written English.
You can use this phrase to refer to something that is in the process of being dissolved, such as a political party or a contract. For example, "The longstanding political party is now under dissolution following a series of internal disputes."
Decrease in pH due to acetogenesis was also modeled, using charge balance equations under CaCO3 dissolution conditions.
Based on the modeling and simulation results, Cmax and AUCt of the venlafaxine openable matrix tablets were entirely within the bioequivalence acceptance limits (i.e., 80%-125%) when the lag time varied from 0 to 4 h and using drug-release profiles under most dissolution conditions.
If SI = 0, there is equilibrium between the mineral and the solution; SI < 0 reflects under saturation (dissolution) with respect to that particular mineral, and SI > 0 oversaturation.
When at least one slice of cells is "defective" under thermal dissolution mechanism, e.g., the oxygen vacancies are occupied by oxygen ions, the reset transition occurs.
We report on new technique for determining and visualization of fluids motion in the vicinity of magnetized ferromagnetic surfaces under chemical dissolution and autocatalytic formation of spatiotemporal structures.
DE is defined as the area under the dissolution curve up to a time t, expressed as a percentage of the area of the rectangle describing 100% dissolution in the same time.
Similar observations showing more sustained supersaturation resulting from a more gradual drug release under nonsink dissolution conditions have also been reported for drug release from swelling clay minerals and ordered mesoporous silica materials in the absence of any crystallization inhibitor.
(6) % DE = ∫ 0 t y × d t y 100 × t × 100 where y is the drug percent dissolved at time t and DE is defined as the area under the dissolution curve up to a certain time, t, expressed as a percentage of the area of the rectangle described by 100% dissolution in the same time (Khan 1975).
Typically, kinetic solubility profiles of ASDs based on conventional water-soluble polymers under nonsink dissolution conditions show an instantaneous dissolution causing an initial surge of drug concentration followed by a sharp decline owing to the nucleation and crystallization events triggered by the rapid buildup of drug supersaturation.
